The UDI Requirements of the New EU MDR – What You Need to Know
The new EU MDR (Medical Device Regulation) changes several aspects of obtaining and then maintaining regulatory approval for medical devices. One of the major changes is the introduction of an identification system, or UDI, for medical devices approved for use in the EU. While the implementation of the new EU MDR has been delayed because … The UDI Requirements of the New EU MDR – What You Need to Know








